Craniofacial Dysostosis

Known as: Crouzon disease, syndrome crouzon's, crouzon's syndrome 
A syndrome inherited in an autosomal dominant pattern. It is characterized by early fusion of the bones of the skull and face. Patients have a… (More)
National Institutes of Health

Papers overview

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Highly Cited
2008
Highly Cited
2008
We have analysed the contributions of neural crest and mesoderm to mammalian craniofacial mesenchyme and its derivatives by cell… (More)
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Highly Cited
2005
Highly Cited
2005
OBJECTIVE Recently, 3-dimensional-computed tomography (3D-CT) imaging has been used in the diagnosis and surgical treatment… (More)
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Highly Cited
2000
Highly Cited
2000
Fibroblast growth factors (FGF) play a critical role in bone growth and development affecting both chondrogenesis and… (More)
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Highly Cited
1996
Highly Cited
1996
Fluconazole has been associated with various teratisms in animals, including craniofacial ossification defects, thin, wavy ribs… (More)
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Highly Cited
1995
Highly Cited
1995
The anterior part of the vertebrate head expresses a group of homeo box genes in segmentally restricted patterns during… (More)
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Highly Cited
1995
Highly Cited
1995
Apert syndrome is a distinctive human malformation comprising craniosynostosis and severe syndactyly of the hands and feet. We… (More)
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Highly Cited
1995
Highly Cited
1995
Dermoids and epidermoids are ectoderm-lined inclusion cysts that differ in complexity: Epidermoids have only squamous epithelium… (More)
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Review
1988
Review
1988
Environmental agents including ethanol, 13-cis retinoic acid (RA, Accutane), the antimetabolite methotrexate, periods of hypoxia… (More)
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Review
1988
Review
1988
Craniofacial mesenchyme is composed of three mesodermal populations - prechordal plate, lateral mesoderm and paraxial mesoderm… (More)
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1988
1988
Ten infants and children who presented with craniofacial dysostosis are discussed; four had Apert's syndrome, four had Crouzon's… (More)
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